Department of Chemical and Biological Physics, Weizmann Institute of Science, 7610001, Rehovot, Israel.
Bruker (UK) Ltd., Banner Lane, Coventry, UK.
Angew Chem Int Ed Engl. 2021 May 17;60(21):11884-11891. doi: 10.1002/anie.202015948. Epub 2021 May 4.
2D NOESY plays a central role in structural NMR spectroscopy. We have recently discussed methods that rely on solvent-driven exchanges to enhance NOE correlations between exchangeable and non-exchangeable protons in nucleic acids. Such methods, however, fail when trying to establish connectivities within pools of labile protons. This study introduces an alternative that also enhances NOEs between such labile sites, based on encoding a priori selected peaks by selective saturations. The resulting selective magnetization transfer (SMT) experiment proves particularly useful for enhancing the imino-imino cross-peaks in RNAs, which is a first step in the NMR resolution of these structures. The origins of these enhancements are discussed, and their potential is demonstrated on RNA fragments derived from the genome of SARS-CoV-2, recorded with better sensitivity and an order of magnitude faster than conventional 2D counterparts.
2D NOESY 在结构 NMR 光谱学中起着核心作用。我们最近讨论了依赖溶剂驱动交换的方法,这些方法可以增强核酸中可交换和不可交换质子之间的 NOE 相关。然而,当试图建立不稳定质子池中的连接时,这些方法会失败。本研究引入了一种替代方法,该方法也可以增强这些不稳定位点之间的 NOE,其基于通过选择性饱和对预先选择的峰进行编码。所得到的选择性磁化转移(SMT)实验对于增强 RNA 中的亚氨基-亚氨基交叉峰特别有用,这是这些结构的 NMR 分辨率的第一步。讨论了这些增强的起源,并在 SARS-CoV-2 基因组衍生的 RNA 片段上证明了它们的潜力,与传统的 2D 对应物相比,该片段的记录具有更好的灵敏度和快一个数量级。